石油与天然气化工
石油與天然氣化工
석유여천연기화공
CHEMICAL ENGINEERING OF OIL AND GAS
2014年
3期
234-240
,共7页
孙敬军%修彭浩%丛日明%董浩%王聪%王雷%刘丹
孫敬軍%脩彭浩%叢日明%董浩%王聰%王雷%劉丹
손경군%수팽호%총일명%동호%왕총%왕뢰%류단
焦化蜡油%碱性氮化物%阳离子活化树脂%固定床%催化裂化
焦化蠟油%堿性氮化物%暘離子活化樹脂%固定床%催化裂化
초화사유%감성담화물%양리자활화수지%고정상%최화열화
coking wax oil%basic nitrogen compounds%cationic activation resin%fixed bed%catalytic cracking
在实验室条件下,分别以D72阳离子活化树脂和D001-CC阳离子活化树脂为吸附剂,在连续吸附固定床反应器中对焦化蜡油进行吸附脱氮研究,并用催化裂化微反装置对脱氮后的焦化蜡油进行催化裂化反应性能研究。考察两种活化树脂在固定床吸附反应器中的吸附穿透曲线、两种活化树脂对焦化蜡油中碱性氮的动态吸附特性及两种活化树脂在不同吸附温度下对焦化蜡油碱性氮脱除率的影响,比较两种活化树脂的吸附性能。脱氮前后焦化蜡油分别进行催化裂化反应,比较脱氮前后焦化蜡油催化裂化反应性能。实验结果表明:D001-CC活化树脂的最佳吸附温度为70℃,6 h后吸附能力达到饱和,饱和吸附量为19.35 m g/g ;D72活化树脂的最佳吸附温度为60℃,5 h后吸附能力达到饱和,饱和吸附量为7.75 m g/g。焦化蜡油经树脂脱氮处理后催化裂化反应程度加深,转化率提高。反应温度为400℃时,未脱氮的焦化蜡油转化率为44%,经过30 m in吸附脱氮处理,焦化蜡油的转化率达到81.5%。在较高的反应温度下,碱性氮的含量对催化剂活性的影响更为敏感,碱性氮的含量减少幅度较大的焦化蜡油,催化裂化的转化率增加更多。
在實驗室條件下,分彆以D72暘離子活化樹脂和D001-CC暘離子活化樹脂為吸附劑,在連續吸附固定床反應器中對焦化蠟油進行吸附脫氮研究,併用催化裂化微反裝置對脫氮後的焦化蠟油進行催化裂化反應性能研究。攷察兩種活化樹脂在固定床吸附反應器中的吸附穿透麯線、兩種活化樹脂對焦化蠟油中堿性氮的動態吸附特性及兩種活化樹脂在不同吸附溫度下對焦化蠟油堿性氮脫除率的影響,比較兩種活化樹脂的吸附性能。脫氮前後焦化蠟油分彆進行催化裂化反應,比較脫氮前後焦化蠟油催化裂化反應性能。實驗結果錶明:D001-CC活化樹脂的最佳吸附溫度為70℃,6 h後吸附能力達到飽和,飽和吸附量為19.35 m g/g ;D72活化樹脂的最佳吸附溫度為60℃,5 h後吸附能力達到飽和,飽和吸附量為7.75 m g/g。焦化蠟油經樹脂脫氮處理後催化裂化反應程度加深,轉化率提高。反應溫度為400℃時,未脫氮的焦化蠟油轉化率為44%,經過30 m in吸附脫氮處理,焦化蠟油的轉化率達到81.5%。在較高的反應溫度下,堿性氮的含量對催化劑活性的影響更為敏感,堿性氮的含量減少幅度較大的焦化蠟油,催化裂化的轉化率增加更多。
재실험실조건하,분별이D72양리자활화수지화D001-CC양리자활화수지위흡부제,재련속흡부고정상반응기중대초화사유진행흡부탈담연구,병용최화열화미반장치대탈담후적초화사유진행최화열화반응성능연구。고찰량충활화수지재고정상흡부반응기중적흡부천투곡선、량충활화수지대초화사유중감성담적동태흡부특성급량충활화수지재불동흡부온도하대초화사유감성담탈제솔적영향,비교량충활화수지적흡부성능。탈담전후초화사유분별진행최화열화반응,비교탈담전후초화사유최화열화반응성능。실험결과표명:D001-CC활화수지적최가흡부온도위70℃,6 h후흡부능력체도포화,포화흡부량위19.35 m g/g ;D72활화수지적최가흡부온도위60℃,5 h후흡부능력체도포화,포화흡부량위7.75 m g/g。초화사유경수지탈담처리후최화열화반응정도가심,전화솔제고。반응온도위400℃시,미탈담적초화사유전화솔위44%,경과30 m in흡부탈담처리,초화사유적전화솔체도81.5%。재교고적반응온도하,감성담적함량대최화제활성적영향경위민감,감성담적함량감소폭도교대적초화사유,최화열화적전화솔증가경다。
Under laboratory conditions ,nitrogen adsorption from the coking wax oil was stud-ied respectively by D72 and D001-CC cationic activation resins as adsorbents in a continuous fixed bed reactor .Micro reaction system of fluid catalytic cracking unit was used to study the catalytic cracking reaction performance of coking wax oil after denitrification .Adsorption properties of two kinds of activation resin were compared by studing the adsorption breakthrough curve in the fixed bed ,the dynamic adsorption properties of alkaline nitrogen compounds in the coking wax oil and the affect of the adsorption temperature on the removal rate of basic nitrogen compounds . Catalytic cracking performances of coking wax oil before and after denitrification were finally compared with catalytic cracking experiments .Results of experiments showed that the optimum adsorption temperature of D001-CC activation resin was 70 ℃ ,the adsorption capacity was satu-rated 6 hours later ,and the saturated adsorption capacity is 19 .35 mg/g .The optimum adsorp-tion temperature of D72 activation resin was 60 ℃ ,the adsorption capacity was saturated 5 hours later ,and the saturated adsorption capacity was 7 .75 mg/g .The degree of catalytic cracking of coking wax oil deepened and the conversion rate improved after dealing with the resin denitrifica-tion .When the reaction temperature was 400 ℃ ,the conversion rate of coking wax oil without denitrification was 44% .The conversion rate of coking wax oil reached 81 .5% after 30 minute’s adsorption denitrification treatment .The influences of alkaline nitrogen content on catalyst activ-ity were more sensitive at higher reaction temperature .The more substantially decrease of alka-line nitrogen content in the coking wax oil ,the more significantly increases of catalytic cracking conversion rates .